| scholarly article | Q13442814 |
| P50 | author | Regine Kahmann | Q1333312 |
| Jan Schirawski | Q64800416 | ||
| P2093 | author name string | Britta Winterberg | |
| Jörg Kämper | |||
| Franziska Lessing | |||
| Philip Müller | |||
| Heiko Eichhorn | |||
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| Cyclic AMP-dependent protein kinase controls virulence of the fungal pathogen Cryptococcus neoformans | Q33968048 | ||
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| Mechanisms of iron regulation in mycobacteria: role in physiology and virulence | Q34182066 | ||
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| Cryptococcus neoformans mating and virulence are regulated by the G-protein alpha subunit GPA1 and cAMP. | Q35197981 | ||
| Analysis of ferrichrome biosynthesis in the phytopathogenic fungus Ustilago maydis: cloning of an ornithine-N5-oxygenase gene | Q35262350 | ||
| Metal-responsive transcription factors that regulate iron, zinc, and copper homeostasis in eukaryotic cells. | Q35661293 | ||
| The yeast A kinases differentially regulate iron uptake and respiratory function. | Q35756462 | ||
| sid1, a gene initiating siderophore biosynthesis in Ustilago maydis: molecular characterization, regulation by iron, and role in phytopathogenicity | Q36080632 | ||
| Identification of a cAMP-dependent protein kinase catalytic subunit required for virulence and morphogenesis in Ustilago maydis | Q36096243 | ||
| Iron uptake from ferrichrome A and iron citrate in Ustilago sphaerogena | Q36331714 | ||
| cAMP regulates morphogenesis in the fungal pathogen Ustilago maydis | Q36730323 | ||
| urbs1, a gene regulating siderophore biosynthesis in Ustilago maydis, encodes a protein similar to the erythroid transcription factor GATA-1. | Q36826150 | ||
| Regulatory networks affected by iron availability in Candida albicans | Q38336209 | ||
| The distal GATA sequences of the sid1 promoter of Ustilago maydis mediate iron repression of siderophore production and interact directly with Urbs1, a GATA family transcription factor | Q38347197 | ||
| Iron uptake in Ustilago maydis: tracking the iron path | Q39565490 | ||
| The siderophore iron transporter of Candida albicans (Sit1p/Arn1p) mediates uptake of ferrichrome-type siderophores and is required for epithelial invasion | Q39656339 | ||
| An unusual MAP kinase is required for efficient penetration of the plant surface by Ustilago maydis | Q39756383 | ||
| PKA and MAPK phosphorylation of Prf1 allows promoter discrimination in Ustilago maydis | Q40240145 | ||
| Mating and pathogenic development of the Smut fungus Ustilago maydis are regulated by one mitogen-activated protein kinase cascade. | Q40495202 | ||
| G proteins in Ustilago maydis: transmission of multiple signals? | Q42615078 | ||
| The b alleles of U. maydis, whose combinations program pathogenic development, code for polypeptides containing a homeodomain-related motif | Q42625846 | ||
| Characterization of iron-binding motifs in Candida albicans high-affinity iron permease CaFtr1p by site-directed mutagenesis | Q43002445 | ||
| Identification of genes in the bW/bE regulatory cascade in Ustilago maydis | Q43818289 | ||
| The ukb1 gene encodes a putative protein kinase required for bud site selection and pathogenicity in Ustilago maydis. | Q44132248 | ||
| The siderophore system is essential for viability of Aspergillus nidulans: functional analysis of two genes encoding l-ornithine N 5-monooxygenase (sidA) and a non-ribosomal peptide synthetase (sidC). | Q44492737 | ||
| Characterization of the ferrichrome A biosynthetic gene cluster in the homobasidiomycete Omphalotus olearius | Q46600230 | ||
| Discrete developmental stages during teliospore formation in the corn smut fungus, Ustilago maydis. | Q46815017 | ||
| Serial Analysis of Gene Expression (SAGE) of Magnaporthe grisea: genes involved in appressorium formation | Q47647030 | ||
| The MAP kinase kpp2 regulates mating and pathogenic development in Ustilago maydis | Q47901505 | ||
| Isolation of a carbon source-regulated gene from Ustilago maydis | Q48056721 | ||
| NPS6, encoding a nonribosomal peptide synthetase involved in siderophore-mediated iron metabolism, is a conserved virulence determinant of plant pathogenic ascomycetes. | Q48083937 | ||
| A two-component regulatory system for self/non-self recognition in Ustilago maydis | Q48185258 | ||
| Characterization of a novel NADH-specific, FAD-containing, soluble reductase with ferric citrate reductase activity from maize seedlings. | Q50519941 | ||
| A reverse genetic approach for generating gene replacement mutants in Ustilago maydis. | Q50795264 | ||
| Activation of the cAMP pathway in Ustilago maydis reduces fungal proliferation and teliospore formation in plant tumors. | Q52163935 | ||
| Identification and complementation of a mutation to constitutive filamentous growth in Ustilago maydis. | Q52516269 | ||
| An oxidase-permease-based iron transport system in Schizosaccharomyces pombe and its expression in Saccharomyces cerevisiae. | Q52523448 | ||
| Iron-regulated transcription and capsule formation in the fungal pathogen Cryptococcus neoformans. | Q52562763 | ||
| Characterization of siderophores from Ustilago maydis. | Q54342361 | ||
| A PCR-based system for highly efficient generation of gene replacement mutants in Ustilago maydis. | Q54737585 | ||
| cAMP UPREGULATES THE TRANSPOSABLE ELEMENT mys-1: A POSSIBLE LINK BETWEEN SIGNALING AND MOBILE DNA | Q58365460 | ||
| Rapid colorimetric micromethod for the quantitation of complexed iron in biological samples | Q68375729 | ||
| A high-affinity iron permease essential for Candida albicans virulence | Q73782663 | ||
| The Ustilago maydis regulatory subunit of a cAMP-dependent protein kinase is required for gall formation in maize | Q73808086 | ||
| The hgl1 gene is required for dimorphism and teliospore formation in the fungal pathogen Ustilago maydis | Q74319624 | ||
| Crosstalk between cAMP and pheromone signalling pathways in Ustilago maydis | Q77715368 | ||
| Environmental signals controlling sexual development of the corn Smut fungus Ustilago maydis through the transcriptional regulator Prf1 | Q77990755 | ||
| The Schizosaccharomyces pombe corepressor Tup11 interacts with the iron-responsive transcription factor Fep1 | Q79359151 | ||
| P433 | issue | 11 | |
| P921 | main subject | corn smut | Q1430040 |
| P304 | page(s) | 3332-3345 | |
| P577 | publication date | 2006-11-30 | |
| P1433 | published in | The Plant Cell | Q3988745 |
| P1476 | title | A ferroxidation/permeation iron uptake system is required for virulence in Ustilago maydis | |
| P478 | volume | 18 |
| Q98177629 | A Novel Factor Essential for Unconventional Secretion of Chitinase Cts1 |
| Q46749955 | A seven-WD40 protein related to human RACK1 regulates mating and virulence in Ustilago maydis |
| Q41940593 | Absence of repellents in Ustilago maydis induces genes encoding small secreted proteins |
| Q39469716 | Adaptation of Ustilago maydis to extreme pH values: A transcriptomic analysis. |
| Q24673498 | An Ustilago maydis gene involved in H2O2 detoxification is required for virulence |
| Q50225493 | An adequate Fe nutritional status of maize suppresses infection and biotrophic growth of Colletotrichum graminicola |
| Q37161425 | An encapsulation of iron homeostasis and virulence in Cryptococcus neoformans. |
| Q28487486 | An extracellular siderophore is required to maintain the mutualistic interaction of Epichloë festucae with Lolium perenne |
| Q104581368 | Apoplastic Proteases: Powerful Weapons against Pathogen Infection in Plants |
| Q37583033 | Assessing the impact of transcriptomics, proteomics and metabolomics on fungal phytopathology. |
| Q30317484 | Biotrophy-specific downregulation of siderophore biosynthesis in Colletotrichum graminicola is required for modulation of immune responses of maize |
| Q39456096 | Differentially regulated high-affinity iron assimilation systems support growth of the various cell types in the dimorphic pathogen Talaromyces marneffei. |
| Q21559506 | Distinct roles for intra- and extracellular siderophores during Aspergillus fumigatus infection |
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| Q37871029 | Fungal pathogenicity genes in the age of 'omics'. |
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| Q34335971 | Genome-wide analysis of copper, iron and zinc transporters in the arbuscular mycorrhizal fungus Rhizophagus irregularis |
| Q36115696 | Genomic Analyses of Cladophialophora bantiana, a Major Cause of Cerebral Phaeohyphomycosis Provides Insight into Its Lifestyle, Virulence and Adaption in Host |
| Q35951401 | HapX Mediates Iron Homeostasis in the Pathogenic Dermatophyte Arthroderma benhamiae but Is Dispensable for Virulence |
| Q84962450 | HapX-mediated iron homeostasis is essential for rhizosphere competence and virulence of the soilborne pathogen Fusarium oxysporum |
| Q28472490 | Histoplasma requires SID1, a member of an iron-regulated siderophore gene cluster, for host colonization |
| Q35220425 | Identification and functional analysis of Penicillium digitatum genes putatively involved in virulence towards citrus fruit |
| Q38619658 | In silico prediction and characterization of secondary metabolite biosynthetic gene clusters in the wheat pathogen Zymoseptoria tritici |
| Q52312721 | In vivo insertion pool sequencing identifies virulence factors in a complex fungal-host interaction. |
| Q35738573 | Iron - A Key Nexus in the Virulence of Aspergillus fumigatus |
| Q53653914 | Iron deficiency affects plant defence responses and confers resistance to Dickeya dadantii and Botrytis cinerea. |
| Q33320198 | Iron source preference and regulation of iron uptake in Cryptococcus neoformans |
| Q45718631 | Isolation and characterisation of a ferrirhodin synthetase gene from the sugarcane pathogen Fusarium sacchari. |
| Q35779263 | Mevalonate governs interdependency of ergosterol and siderophore biosyntheses in the fungal pathogen Aspergillus fumigatus |
| Q35084750 | Multiple multi-copper oxidase gene families in basidiomycetes - what for? |
| Q53698735 | No effects without causes: the Iron Dysregulation and Dormant Microbes hypothesis for chronic, inflammatory diseases. |
| Q39254552 | Physical and functional interaction of FgFtr1-FgFet1 and FgFtr2-FgFet2 is required for iron uptake in Fusarium graminearum |
| Q35208207 | Plant surface cues prime Ustilago maydis for biotrophic development |
| Q37374730 | Role of ferroxidases in iron uptake and virulence of Cryptococcus neoformans. |
| Q38061497 | Role of iron homeostasis in the virulence of phytopathogenic bacteria: an 'à la carte' menu. |
| Q43189811 | Roles of iron in plant defence and fungal virulence |
| Q42103491 | Salicylic acid, yersiniabactin, and pyoverdin production by the model phytopathogen Pseudomonas syringae pv. tomato DC3000: synthesis, regulation, and impact on tomato and Arabidopsis host plants |
| Q30318865 | Sfp-type 4'-phosphopantetheinyl transferase is indispensable for fungal pathogenicity |
| Q37009518 | Siderophore Biosynthesis but Not Reductive Iron Assimilation Is Essential for the Dimorphic Fungus Nomuraea rileyi Conidiation, Dimorphism Transition, Resistance to Oxidative Stress, Pigmented Microsclerotium Formation, and Virulence |
| Q27976506 | SreA-mediated iron regulation in Aspergillus fumigatus |
| Q88427265 | The Role of Iron Competition in the Antagonistic Action of the Rice Endophyte Streptomyces sporocinereus OsiSh-2 Against the Pathogen Magnaporthe oryzae |
| Q34291040 | The Sfp-type 4'-phosphopantetheinyl transferase Ppt1 of Fusarium fujikuroi controls development, secondary metabolism and pathogenicity |
| Q56970871 | The Top 10 fungal pathogens in molecular plant pathology |
| Q34637164 | The Top 10 fungal pathogens in molecular plant pathology |
| Q42601041 | The Ustilago maydis Nit2 homolog regulates nitrogen utilization and is required for efficient induction of filamentous growth |
| Q36419997 | The cAMP/protein kinase A signaling pathway in pathogenic basidiomycete fungi: Connections with iron homeostasis |
| Q33892459 | The complete genome sequence of 'Candidatus Liberibacter solanacearum', the bacterium associated with potato zebra chip disease |
| Q40376418 | The ectomycorrhizal basidiomycete Hebeloma cylindrosporum undergoes early waves of transcriptional reprogramming prior to symbiotic structures differentiation |
| Q45091061 | The ferrous iron transporter FtrABCD is required for the virulence of Brucella abortus 2308 in mice |
| Q34016251 | The general transcriptional repressor Tup1 is required for dimorphism and virulence in a fungal plant pathogen |
| Q38647323 | The metalloreductase FreB is involved in adaptation of Aspergillus fumigatus to iron starvation. |
| Q52601066 | The siderophore biosynthetic gene SID1, but not the ferroxidase gene FET3, is required for full Fusarium graminearum virulence. |
| Q41966460 | The transcription factor Rbf1 is the master regulator for b-mating type controlled pathogenic development in Ustilago maydis |
| Q53304907 | TheUstilago maydisClp1 Protein Orchestrates Pheromone andb-Dependent Signaling Pathways to Coordinate the Cell Cycle and Pathogenic Development |
| Q44969847 | Transcriptome analysis of Stagonospora nodorum: gene models, effectors, metabolism and pantothenate dispensability |
| Q35587757 | Transcriptome analysis of cyclic AMP-dependent protein kinase A-regulated genes reveals the production of the novel natural compound fumipyrrole by Aspergillus fumigatus |
| Q59794992 | Transcripts and tumors: regulatory and metabolic programming during biotrophic phytopathogenesis |
| Q40165745 | White collar 1-induced photolyase expression contributes to UV-tolerance of Ustilago maydis. |
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